AIROS 6P Sequential Compression Device— 510(k) K223195

Substantially Equivalent

Airos Medical, Inc.

FDA 510(k) clearance K223195 for AIROS 6P Sequential Compression Device, Substantially Equivalent on 2022-12-09. Applicant: Airos Medical, Inc..

Clearance details

Applicant: Airos Medical, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2022-10-13
Decision date: 2022-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Audubon, PA, US

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